132541-62-9 Usage
Uses
Used in Pharmaceutical Industry:
15,15'-epoxy-beta,beta-carotene is used as a provitamin A compound for its ability to be converted into vitamin A in the human body. This conversion plays a crucial role in maintaining healthy vision, supporting the immune system, and promoting proper growth and development.
Used in Nutraceutical Industry:
In the nutraceutical industry, 15,15'-epoxy-beta,beta-carotene is used as a dietary supplement for its antioxidant properties. It helps to neutralize free radicals, reducing the risk of chronic diseases and promoting overall health.
Used in Cosmetic Industry:
15,15'-epoxy-beta,beta-carotene is used as a natural colorant in the cosmetic industry due to its vibrant orange hue. It is a safer alternative to synthetic colorants and is often used in lip products, creams, and other skincare formulations.
Used in Food Industry:
In the food industry, 15,15'-epoxy-beta,beta-carotene is used as a natural color additive to enhance the appearance of various products, such as juices, snacks, and confectionery items. Its natural origin and health benefits make it a preferred choice over synthetic colorants.
Used in Agricultural Industry:
15,15'-epoxy-beta,beta-carotene is used in the agricultural industry as a feed additive to improve the color and nutritional value of animal products, such as egg yolks and fish flesh. This enhances the marketability and health benefits of these products for consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 132541-62-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,4 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 132541-62:
(8*1)+(7*3)+(6*2)+(5*5)+(4*4)+(3*1)+(2*6)+(1*2)=99
99 % 10 = 9
So 132541-62-9 is a valid CAS Registry Number.
132541-62-9Relevant articles and documents
Oxidative degradation of β-carotene and β-apo-8′-carotenal
Mordi, Raphael C.,Walton, John C.,Burton, Graham W.,Hughes, Lise,Ingold U., Keith,Lindsay A., David,Moffatt J., Douglas
, p. 911 - 928 (2007/10/02)
In the self-initiated oxidation of β-carotene with molecular oxygen the rate of oxygen uptake was shown to depend on the oxygen partial pressure. Epoxides, dihydrofurans, carbonyl compounds, carbon dioxide, oligomeric material, traces of alcohols, and probably carboxylic acids were formed. The main products in the early stage of the oxidation were shown to be 5,6-epoxy-β-carotene. 15,15′-epoxy-′-carotene, diepoxides, and a series of β-apo-carotenals and -carotenones. As the oxidation proceeded uncharacterised oligomeric material and the carbonyl compounds became more important and the epoxides degraded. In the final phase of the oxidation the longer chain β-apo-carotenals were themselves oxidized to shorter chain carbonyl compounds, particularly β-apo-13-carotenone, β-ionone, 5,6-epoxy-gb-ionone, dihydroactinidiolide and probably carboxylic acids. The effect of iron, copper and zinc stearates on the product composition and proportions was studied, as was the effect of light. The oxidation was inhibited by 2,6-di-t-butyl-4-methyphenol and α-tocopherol. The oxidations of β-apo-8′-carotenal and retinal under similar conditions were studied briefly, and the main products from the former compound were characterized. The initiation, the formation of the epoxides, the β-apo-carotenals and -carotenones, the successive chain shortening of the aldehydes to the ketones, and the formation of dihydroactinidiolide are explained in terms of free radical peroxidation chemistry.
